autosomal recessive nonsyndromic deafness 21

Term ID

DOID:0110479

Synonyms

• autosomal recessive deafness 21
• DFNB21

Definition

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23.3. https://www.ncbi.nlm.nih.gov/pubmed/9949200

References

• ICD10CM:H90.3
• MIM:603629

Ontology

Human Disease   ( DOID:0110479 )